Canonical Allele Identifier: CA2840996408

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824750C>A , CM000671.2:g.127824750C>A	GRCh38
NC_000009.11:g.130587029C>A , CM000671.1:g.130587029C>A	GRCh37
NC_000009.10:g.129626850C>A	NCBI36
NG_009551.1:g.35019G>T , LRG_589:g.35019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.445+50G>T	ENSP00000479015.1:n.445+50G>T
ENST00000373203.9:c.991+50G>T MANE Select	ENSP00000362299.4:n.991+50G>T
ENST00000344849.4:c.991+50G>T	ENSP00000341917.3:n.991+50G>T
ENST00000373203.8:c.991+50G>T	ENSP00000362299.4:n.991+50G>T
ENST00000480266.5:c.445+50G>T	ENSP00000479015.1:n.445+50G>T
NM_000118.3:c.991+50G>T , LRG_589t1:c.991+50G>T	NP_000109.1:n.991+50G>T
NM_001114753.2:c.991+50G>T , LRG_589t2:c.991+50G>T	NP_001108225.1:n.991+50G>T
NM_001278138.1:c.445+50G>T	NP_001265067.1:n.445+50G>T
NM_001114753.3:c.991+50G>T MANE Select	NP_001108225.1:n.991+50G>T
NM_001278138.2:c.445+50G>T	NP_001265067.1:n.445+50G>T